Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4809 |
| ensemblid | ENSG00000100138.15 |
| hgncid | 7819 |
| symbol | SNU13 |
| name | small nuclear ribonucleoprotein 13 |
| refseq_nuc | NM_001003796.2 |
| refseq_prot | NP_001003796.1 |
| ensembl_nuc | ENST00000401959.6 |
| ensembl_prot | ENSP00000383949.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41673933 |
| end | 41688867 |
| strand | - |
| ver | v1.2 |
| region | chr22:41673933-41688867 |
| region5000 | chr22:41668933-41693867 |
| regionname0 | SNU13_chr22_41673933_41688867 |
| regionname5000 | SNU13_chr22_41668933_41693867 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 384 | 359 | 83 | 68 | 147 | 16 | 43 | SNU13_chr22_41668933_41693867 | SNU13 | ATGAC others(379): Show |
chr22 | 41668933 | 41693867 | ||
| a0001c0002 | 0/0 | 384 | 17 | 5 | 4 | 7 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | ATGAC others(379): Show |
chr22 | 41668933 | 41693867 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1458 | 258 | 65 | 50 | 107 | 8 | 27 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0002 | 0/0 | 1458 | 74 | 2 | 13 | 40 | 5 | 14 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0003 | 0/0 | 1458 | 10 | 7 | 3 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0004 | 0/0 | 1458 | 6 | 6 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0005 | 0/0 | 1458 | 5 | 0 | 2 | 0 | 3 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0006 | 0/0 | 1458 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0007 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGATG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0008 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0009 | 0/1 | 1458 | 1 | 0 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0001t0010 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| a0001c0002t0001 | 0/0 | 1458 | 17 | 5 | 4 | 7 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | CGGTG others(1453): Show |
chr22 | 41668933 | 41693867 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 48 | 4 | 12 | 24 | 2 | 6 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0002 | 1/0 | 47 | 1 | 20 | 11 | 3 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0004 | 0/0 | 39 | 3 | 1 | 34 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0003 | 0/0 | 44 | 1 | 10 | 17 | 5 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0003g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0004g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0005g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0009g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0001t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0092 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0091 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CDX | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0109 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | GIH | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0114 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0110 | REF | REF | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41680326 | G | A | 1 | a0001c0002 | 17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
synonymous_variant | LOW | c.42C>T | p.Ala14Ala | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/3 | 113/1458 | 42/387 | 14/128 | chr22 | 41680326 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41673996 | C | G | 2 | a0001c0001t0004 a0001c0001t0010 |
7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 937 | chr22 | 41673996 | ||||||
| chr22:41674223 | G | A | 1 | a0001c0001t0003 | 10 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*710C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 710 | chr22 | 41674223 | ||||||
| chr22:41674272 | T | C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*661A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 661 | chr22 | 41674272 | ||||||
| chr22:41674313 | G | A | 2 | a0001c0001t0004 a0001c0001t0010 |
7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*620C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 620 | chr22 | 41674313 | ||||||
| chr22:41674370 | A | C | 1 | a0001c0001t0005 | 5 | HG00733.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*563T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 563 | chr22 | 41674370 | ||||||
| chr22:41674512 | A | G | 1 | a0001c0001t0006 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*421T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 421 | chr22 | 41674512 | ||||||
| chr22:41674625 | C | T | 1 | a0001c0001t0008 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 308 | chr22 | 41674625 | ||||||
| chr22:41674789 | C | T | 1 | a0001c0001t0002 | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*144G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 144 | chr22 | 41674789 | ||||||
| chr22:41674818 | T | C | 1 | a0001c0001t0004 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*115A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 115 | chr22 | 41674818 | ||||||
| chr22:41674859 | A | G | 1 | a0001c0001t0004 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 74 | chr22 | 41674859 | ||||||
| chr22:41688865 | C | T | 1 | a0001c0001t0007 | 1 | HG02145.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/3 | chr22 | 41688865 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41675568 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.125-373G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675568 | |||||||
| chr22:41675580 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.125-385A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675580 | |||||||
| chr22:41675744 | CT | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(6): Show |
22 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.125-550delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675744 | |||||||
| chr22:41675754 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0116 |
4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-559A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675754 | |||||||
| chr22:41675826 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0058 others(2): Show |
7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-631A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675826 | |||||||
| chr22:41675845 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0025 others(11): Show |
25 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.125-650C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675845 | |||||||
| chr22:41676150 | T | A | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-955A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676150 | |||||||
| chr22:41676152 | T | A | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-957A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676152 | |||||||
| chr22:41676445 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.125-1250G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676445 | |||||||
| chr22:41676456 | C | A | 1 | a0001c0001t0006g0038 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.125-1261G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676456 | |||||||
| chr22:41676531 | C | CT | 14 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(11): Show |
42 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.125-1337dupA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676531 | |||||||
| chr22:41676531 | CT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(67): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.125-1337delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676531 | |||||||
| chr22:41676814 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1619G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676814 | |||||||
| chr22:41676849 | T | C | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-1654A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676849 | |||||||
| chr22:41676908 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(96): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.125-1713G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676908 | |||||||
| chr22:41676931 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.125-1736A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676931 | |||||||
| chr22:41677059 | G | C | 23 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(20): Show |
51 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.125-1864C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677059 | |||||||
| chr22:41677130 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.125-1935G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677130 | |||||||
| chr22:41677153 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0111 |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1958G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677153 | |||||||
| chr22:41677154 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125-1959G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677154 | |||||||
| chr22:41677240 | T | C | 1 | a0001c0002t0001g0020 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.125-2045A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677240 | |||||||
| chr22:41677394 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-2199C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677394 | |||||||
| chr22:41677512 | T | A | 1 | a0001c0001t0001g0035 | 2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.125-2317A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677512 | |||||||
| chr22:41677828 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0025 others(11): Show |
25 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.124+2416G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677828 | |||||||
| chr22:41677979 | C | CT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0021 others(8): Show |
30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.124+2264dupA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677979 | |||||||
| chr22:41677979 | C | CTT | 3 | a0001c0001t0002g0056 a0001c0001t0004g0010 a0001c0001t0010g0114 |
7 | HG01175.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+2263_124+2264d others(4): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677979 | |||||||
| chr22:41677998 | C | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+2246G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677998 | |||||||
| chr22:41678018 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+2226G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678018 | |||||||
| chr22:41678038 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.124+2206T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678038 | |||||||
| chr22:41678044 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0049 |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+2200G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678044 | |||||||
| chr22:41678124 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0090 |
3 | HG02145.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+2120G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678124 | |||||||
| chr22:41678210 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(96): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.124+2034G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678210 | |||||||
| chr22:41678211 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(100): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.124+2033T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678211 | |||||||
| chr22:41678226 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0016 others(30): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.124+2018G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678226 | |||||||
| chr22:41678305 | A | G | 1 | a0001c0001t0003g0006 | 9 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1939T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678305 | |||||||
| chr22:41678405 | A | G | 1 | a0001c0001t0008g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124+1839T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678405 | |||||||
| chr22:41678474 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124+1770T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678474 | |||||||
| chr22:41678591 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0066 |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+1653A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678591 | |||||||
| chr22:41678724 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.124+1520G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678724 | |||||||
| chr22:41678745 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(2): Show |
18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.124+1499C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678745 | |||||||
| chr22:41678770 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.124+1474T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678770 | |||||||
| chr22:41678875 | A | C | 1 | a0001c0001t0001g0013 | 5 | HG02965.hp1 HG03130.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+1369T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678875 | |||||||
| chr22:41678950 | A | T | 3 | a0001c0001t0004g0010 a0001c0001t0004g0049 a0001c0001t0010g0114 |
7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1294T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678950 | |||||||
| chr22:41679079 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0053 |
2 | HG01346.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.124+1165C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679079 | |||||||
| chr22:41679139 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0108 |
2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.124+1105A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679139 | |||||||
| chr22:41679296 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(69): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.124+948C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679296 | |||||||
| chr22:41679422 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0081 |
3 | HG00673.hp1 NA18990.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.124+822C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679422 | |||||||
| chr22:41679577 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(93): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.124+667A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679577 | |||||||
| chr22:41679677 | GCT | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0029 |
4 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+565_124+566del others(2): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679677 | |||||||
| chr22:41679678 | CTT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(100): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.124+564_124+565del others(2): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679678 | |||||||
| chr22:41679996 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124+248G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679996 | |||||||
| chr22:41680159 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0079 |
2 | HG02015.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.124+85G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41680159 | |||||||
| chr22:41680377 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(96): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4-13G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680377 | |||||||
| chr22:41680637 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(96): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4-273T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680637 | |||||||
| chr22:41680685 | T | C | 1 | a0001c0001t0008g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-321A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680685 | |||||||
| chr22:41680858 | C | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(2): Show |
18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-494G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680858 | |||||||
| chr22:41680893 | C | T | 1 | a0001c0001t0010g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4-529G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680893 | |||||||
| chr22:41680952 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(96): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4-588G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680952 | |||||||
| chr22:41680964 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(2): Show |
18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-600C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680964 | |||||||
| chr22:41680985 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-621C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680985 | |||||||
| chr22:41681104 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0099 |
2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.4-740C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681104 | |||||||
| chr22:41681176 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0107 |
3 | NA18957.hp2 NA18977.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4-812T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681176 | |||||||
| chr22:41681733 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.4-1369T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681733 | |||||||
| chr22:41681854 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(68): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.4-1490C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681854 | |||||||
| chr22:41681919 | A | T | 1 | a0001c0001t0001g0033 | 2 | NA18986.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4-1555T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681919 | |||||||
| chr22:41681935 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4-1571G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681935 | |||||||
| chr22:41681965 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4-1601C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681965 | |||||||
| chr22:41681990 | CT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.4-1627delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681990 | |||||||
| chr22:41682030 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4-1666C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682030 | |||||||
| chr22:41682155 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4-1791G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682155 | |||||||
| chr22:41682156 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-1792C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682156 | |||||||
| chr22:41682201 | T | C | 1 | a0001c0001t0008g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-1837A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682201 | |||||||
| chr22:41682359 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4-1995T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682359 | |||||||
| chr22:41682449 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4-2085C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682449 | |||||||
| chr22:41682453 | G | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2089C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682453 | |||||||
| chr22:41682509 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4-2145C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682509 | |||||||
| chr22:41682662 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(69): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4-2298T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682662 | |||||||
| chr22:41682788 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0111 others(1): Show |
10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4-2424T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682788 | |||||||
| chr22:41682800 | C | G | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2436G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682800 | |||||||
| chr22:41682805 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2441G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682805 | |||||||
| chr22:41682933 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2569C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682933 | |||||||
| chr22:41683008 | T | G | 1 | a0001c0001t0002g0101 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4-2644A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683008 | |||||||
| chr22:41683012 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4-2648A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683012 | |||||||
| chr22:41683030 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4-2666G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683030 | |||||||
| chr22:41683042 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0049 |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-2678G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683042 | |||||||
| chr22:41683153 | C | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(5): Show |
25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-2789G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683153 | |||||||
| chr22:41683154 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(5): Show |
25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-2790C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683154 | |||||||
| chr22:41683162 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4-2798T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683162 | |||||||
| chr22:41683235 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0066 |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-2871T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683235 | |||||||
| chr22:41683236 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4-2872C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683236 | |||||||
| chr22:41683242 | C | T | 2 | a0001c0001t0003g0006 a0001c0001t0003g0045 |
10 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-2878G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683242 | |||||||
| chr22:41683309 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4-2945G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683309 | |||||||
| chr22:41683357 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
4 | HG00639.hp1 HG02735.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2993C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683357 | |||||||
| chr22:41683665 | A | T | 2 | a0001c0001t0005g0091 a0001c0001t0005g0092 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4-3301T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683665 | |||||||
| chr22:41683728 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4-3364C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683728 | |||||||
| chr22:41683730 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(68): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.4-3366C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683730 | |||||||
| chr22:41683900 | T | TG | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-3537_4-3536insC | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683900 | |||||||
| chr22:41683902 | T | G | 1 | a0001c0001t0001g0017 | 3 | HG03225.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4-3538A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683902 | |||||||
| chr22:41684060 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4-3696G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684060 | |||||||
| chr22:41684076 | G | C | 1 | a0001c0002t0001g0014 | 4 | HG00408.hp2 HG00423.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-3712C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684076 | |||||||
| chr22:41684184 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(94): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.4-3820A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684184 | |||||||
| chr22:41684266 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-3902C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684266 | |||||||
| chr22:41684293 | G | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(5): Show |
25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-3929C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684293 | |||||||
| chr22:41684472 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4-4108G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684472 | |||||||
| chr22:41684528 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4-4164A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684528 | |||||||
| chr22:41684769 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0111 others(1): Show |
10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+4025C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684769 | |||||||
| chr22:41684796 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+3998C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684796 | |||||||
| chr22:41684799 | T | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+3995A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684799 | |||||||
| chr22:41684926 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3+3868C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684926 | |||||||
| chr22:41684951 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3+3843A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684951 | |||||||
| chr22:41684985 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3+3809C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684985 | |||||||
| chr22:41685059 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(69): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.3+3735C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685059 | |||||||
| chr22:41685086 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3+3708G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685086 | |||||||
| chr22:41685154 | C | CA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(8): Show |
25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.3+3639dupT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | |||||||
| chr22:41685154 | C | CAA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(80): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3+3638_3+3639dupTT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | |||||||
| chr22:41685154 | C | CAAA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0080 others(3): Show |
12 | HG00597.hp2 HG01175.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+3637_3+3639dupTT others(1): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | |||||||
| chr22:41685246 | G | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+3548C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685246 | |||||||
| chr22:41685247 | C | A | 1 | a0001c0001t0010g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+3547G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685247 | |||||||
| chr22:41685593 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0059 |
2 | NA18942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.3+3201G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685593 | |||||||
| chr22:41685599 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+3195T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685599 | |||||||
| chr22:41685616 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+3178G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685616 | |||||||
| chr22:41685693 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+3101A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685693 | |||||||
| chr22:41685704 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3+3090C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685704 | |||||||
| chr22:41685711 | A | T | 1 | a0001c0001t0008g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+3083T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685711 | |||||||
| chr22:41685731 | T | C | 6 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0020 others(3): Show |
17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+3063A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685731 | |||||||
| chr22:41685760 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3+3034C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685760 | |||||||
| chr22:41685779 | A | G | 4 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0113 others(1): Show |
13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+3015T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685779 | |||||||
| chr22:41685845 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0111 |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+2949C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685845 | |||||||
| chr22:41685917 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+2877T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685917 | |||||||
| chr22:41685968 | CA | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(86): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3+2825delT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685968 | |||||||
| chr22:41685968 | CAA | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0058 others(5): Show |
10 | HG01167.hp2 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+2824_3+2825delTT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685968 | |||||||
| chr22:41686115 | C | T | 1 | a0001c0001t0010g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+2679G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686115 | |||||||
| chr22:41686127 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3+2667C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686127 | |||||||
| chr22:41686155 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3+2639C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686155 | |||||||
| chr22:41686243 | T | G | 6 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0020 others(3): Show |
17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+2551A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686243 | |||||||
| chr22:41686304 | CT | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0032 others(6): Show |
15 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3+2489delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686304 | |||||||
| chr22:41686325 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0016 others(34): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.3+2469C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686325 | |||||||
| chr22:41686429 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0112 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+2365G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686429 | |||||||
| chr22:41686493 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+2301A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686493 | |||||||
| chr22:41686497 | G | T | 1 | a0001c0001t0002g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3+2297C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686497 | |||||||
| chr22:41686712 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG01884.hp1 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+2082G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686712 | |||||||
| chr22:41686713 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3+2081C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686713 | |||||||
| chr22:41686787 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3+2007A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686787 | |||||||
| chr22:41686964 | T | G | 1 | a0001c0001t0008g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+1830A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686964 | |||||||
| chr22:41687025 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG00099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3+1769C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687025 | |||||||
| chr22:41687041 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0049 |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+1753G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687041 | |||||||
| chr22:41687087 | G | A | 3 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0117 |
12 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1707C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687087 | |||||||
| chr22:41687113 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3+1681G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687113 | |||||||
| chr22:41687123 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3+1671T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687123 | |||||||
| chr22:41687161 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0111 others(1): Show |
10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+1633C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687161 | |||||||
| chr22:41687333 | A | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0044 others(2): Show |
18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.3+1461T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687333 | |||||||
| chr22:41687403 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0043 |
6 | HG00735.hp2 HG01074.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1391G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687403 | |||||||
| chr22:41687603 | T | C | 1 | a0001c0001t0006g0038 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3+1191A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687603 | |||||||
| chr22:41687762 | T | C | 6 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0020 others(3): Show |
17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+1032A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687762 | |||||||
| chr22:41687825 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3+969C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687825 | |||||||
| chr22:41687827 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3+967T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687827 | |||||||
| chr22:41687924 | G | A | 1 | a0001c0001t0010g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+870C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687924 | |||||||
| chr22:41687962 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3+832C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687962 | |||||||
| chr22:41688076 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0116 |
4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+718G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688076 | |||||||
| chr22:41688130 | G | C | 1 | a0001c0001t0002g0039 | 2 | NA18979.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.3+664C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688130 | |||||||
| chr22:41688233 | T | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0117 |
12 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+561A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688233 | |||||||
| chr22:41688391 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3+403C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688391 | |||||||
| chr22:41688478 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+316G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688478 | |||||||
| chr22:41688659 | T | G | 1 | a0001c0001t0002g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3+135A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688659 |